Physio Control Lifepak CR2 Replacement Electrode Kit
Physio Control Lifepak CR2 Replacement Electrode Kit
Product Code 11101-000021ie
- Replacement Electrode Kit for Lifepak CR2 defibrillator
This replacement electrode kit is for use with the Physio Control Lifepak CR2 defibrillator range. The CR2 boasts many new innovations for the AED industry, including cprINSIGHT™ which allows the defibrillator to analyse the patient’s heart rhythm whilst CPR is being delivered, making it the first defibrillator to make a shock or no shock advised decision alongside CPR delivery.
As many of you are aware, electrode pads are one use only and because of this, we highly recommend you have a spare pair on standby so your device is always rescue ready, should there be a cardiac emergency.
Changing electrode pads to paediatric pads is a thing of the past thanks to the Lifepak CR2’s paediatric switch. These electrode pads can be used on both adults and children. This assists with treatment being delivered as quickly as possible, as well as with on-going costs to run the defibrillator.
About the Lifepak CR2
The Physio Control Lifepak CR2 has been designed with low maintenance in mind, allowing you to manage your defibrillator device remotely, online through the all new Online Management System, LIFELINKcentral™.
LIFELINKcentral™ provides you with regular updates about the status of your AED, including notifications 90,60 and 30 days prior to your add-ons expiring, allowing you plenty of time to get your replacement add-ons purchased. If your defibrillator requires attention, then you will be alerted in due time.
This piece of software makes AED maintenance simple and accurate, removing the risk of human error and creating one of the most cost effective defibrillators available on the market.
After you have purchased your replacement electrode pads, LIFELINKcentral™ will automatically update with the new expiry dates displayed, ensuring consistent, accurate information.
If you would like more information about the replacement electrode pad kit for the Physio Control Lifepak CR2, the friendly defibshop team are here to help.
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Buying a defibrillator? You’ve come to the right place...
- With nearly 20 different defibrillator models available, our defibshop team knows them all and can help you decide which device suits your budget, environment and business
- We have over 20 staff on hand who can offer friendly and impartial advice on all things defibrillators
- Not only do we provide a free battery and electrode pad reminder service, but we will replace your electrode pads for free if they are used within two years of purchase
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We were recently listed in the Small Business category of the 'Great Place to Work: Best Workplaces 2014’ whilst we have also won accolades in the Salford Business Awards 2014 & 2012, Investors in People Bronze award and an Insight 100 Customer Service Award in Training Services 2013.
What is an IP rating?
An IP (Ingress Protection) rating classifies the degrees of protection of an electrical item against water and dust. Beginning with IP and followed by two numbers, the first digit is indicative of the item’s resistance to dust and the second is of its resistance to water. Protection against dust is measured from */ 0 up to 6, whereas protection against water is measured from */ 0 up to 8. The protection against these elements increases as the number does, with * / 0 telling us that the item has NO protection against either dust or water.
Why is this important?
The IP rating of a defib will tell you (and us!) whether it is suitable for the environment where it’s most likely to be used; for example, if there is a good chance your defib may be used in an outdoor environment, you will need a unit with a higher IP rating to ensure it can be used regardless the weather or terrain. If you are looking for a defibrillator more suitable for an indoors environment, you can afford to choose one with a lower IP rating, based on the other features that may be more suitable.
When a particular product is “approved” by the FDA, this marks the pass in the premarket approval (or PMA) application of a particular product which has been submitted to the FDA.
To receive approval of a device through a PMA application, the applicant in question must provide reasonable assurance of the device’s safety and effectiveness which is then challenged by the FDA before being approved.
Whilst all AEDs can be used to increase chances of survival and even save a life in the event of a cardiac arrest, FDA approved devices provide that extra piece of mind that the specific unit being used has undergone vigorous and substantial testing to ensure that that particular piece of equipment operates just as it should and provides the most effective care possible.
Many manufacturers perform their own tests on products, but not all defibrillators will undergo the same premarket approval as FDA approved devices and there is no guarantee or stamp of certification if testing has taken place with non-FDA approved products.